转胺酶为选择性M1/M4激动剂的合成提供了关键的状构建块
Christopher G Thomson1, Kelly Boss1, Amy Calhoun1
1Global Discovery Chemistry, Novartis Biomedical Research, Cambridge, Massachusetts 02139, United States.
ACS medicinal chemistry letters
|December 20, 2023
概括
研究人员使用生物催化剂为肌肉酸M4激动剂创造了一种新的合合成方法. 这种方法有效地产生了关键的螺旋环二胺,从而发现了选择性的M1/M4激动剂.
科学领域:
- 药用化学 医学化学
- 有机合成 有机合成
- 生物催化剂是一种生物催化剂.
背景情况:
- 肌肉M4激动剂是重要的治疗点.
- 效率高的合成奇拉螺旋环二胺是具有挑战性的.
- 开发选择性的M1/M4激动剂需要新的合成策略.
研究的目的:
- 开发一种向肌性M4激动剂的性合成途径.
- 为了利用生物催化剂合成关键的螺旋环二胺构建块.
- 通过药物化学的努力来确定选择性的M1/M4激动剂.
主要方法:
- 螺旋环二胺构建块的生物催化合成 (10和12).
- 使用双功能二胺中间体,优化合成序列.
- 早期的药用化学探索使用先进的中间体.
主要成果:
- 成功开发了一条向肌性M4激动剂的性途径.
- 通过生物催化剂有效合成关键的螺旋环二胺构建块.
- 选择性M1/M4激动剂的鉴定.
结论:
- 由生物催化剂启用的开发的性途径,有效合成肌肉酸M4激活剂.
- 双功能螺旋环二胺是药物化学的有价值的中间体.
- 这种方法有助于发现选择性M1/M4激动剂.
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